材料科学
超级电容器
微型多孔材料
化学工程
碳纤维
氢氧化钾
氢氧化铵
石墨烯
吸附
氮气
石墨氮化碳
发泡剂
无机化学
电容
纳米技术
有机化学
复合材料
物理化学
化学
催化作用
聚氨酯
工程类
复合数
光催化
电极
作者
Siddulu Naidu Talapaneni,Ji Hoon Lee,Sang Hyun Je,Onur Büyükçakır,TaeWoo Kwon,Kyriaki Polychronopoulou,Jang Wook Choi,Ali Coşkun
标识
DOI:10.1002/adfm.201604658
摘要
A scalable, template‐free synthetic strategy is presented for the preparation of ultramicroporous carbon nitride frameworks (CNFs) through a chemical blowing approach by using ammonium chloride as blowing agent and hexamethylene tetraamine as the C and N precursor and a subsequent potassium hydroxide chemical activation is employed to obtain CNFs with surface areas up to 1730 m 2 g −1 along with a high nitrogen content of 13.3 wt%. CNFs showed CO 2 uptake capacities up to 5.74 mmol g −1 at 1 bar and 1.67 mmol g −1 at 0.15 bar, 273 K along with a very high CO 2 /N 2 selectivity. In addition, H 2 uptake capacity of 1.9 wt% and the isosteric heats of adsorption ( Q st ) value of 9.0 kJ mol −1 at zero coverage have been also observed. Moreover, the presence of nitrogen‐doped graphene walls in CNFs also facilitated their application as supercapacitors, with capacitance values up to ≈114 F g −1 at 0.5 A g −1 , along with a good cyclability and capacitance retention. This approach effectively extends unique surface properties of carbon nitrides into the micropore regime for effective capture of small gases and energy storage applications. Importantly, textural properties of CNFs can be simply tuned by judicious choice of organic precursors and the blowing agent.
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